In vivo imaging of reactive oxygen and nitrogen species in inflammation using the luminescent probe L-012Show others and affiliations
2009 (English)In: Free Radical Biology & Medicine, ISSN 0891-5849, E-ISSN 1873-4596, Vol. 47, no 6, p. 760-766Article in journal (Refereed) Published
Abstract [en]
Production of reactive oxygen and nitrogen species (ROS/RNS) is an important part of the inflammatory response, but prolonged elevated levels of ROS/RNS as under chronic inflammation can contribute to the development of disease. Monitoring ROS/RNS in living animals is challenging due to the rapid turnover of ROS/RNS and the limited sensitivity and specificity of ROS/RNS probes. We have explored the use of the chemiluminescent probe L-012 for noninvasive imaging of ROS/RNS production during inflammation in living mice. Various inflammatory conditions were induced, and L-012-dependent luminescence was recorded with an ultrasensitive CCD camera. Strong luminescent signals were observed from different regions of the body corresponding to inflammation. The signal was reduced by administration of the SOD mimetic tempol, the NADPH oxidase inhibitor apocynin, and the inhibitor of nitric oxide synthesis L-NAME, signifying the requirement for the presence of ROS/RNS. Additionally, the L-012 signal was abolished in mice with a mutation in the Ncf1 gene, encoding a protein in the NADPH oxidase complex 2, which generates ROS/RNS during inflammation. In conclusion, L-012 is well distributed in the mouse body and mediates a strong ROS/RNS-dependent luminescent signal in vivo and is useful for monitoring the development and regulation of inflammation in living organisms. © 2009 Elsevier Inc. All rights reserved.
Place, publisher, year, edition, pages
Philadelphia, PA: Elsevier, 2009. Vol. 47, no 6, p. 760-766
Keywords [en]
Chemiluminescence, Free radical, In vivo, Inflammation, L-012, Luminescence, Molecular imaging, Mouse, Optical imaging, RNS, ROS
National Category
Cell and Molecular Biology
Identifiers
URN: urn:nbn:se:hh:diva-48851DOI: 10.1016/j.freeradbiomed.2009.06.013ISI: 000273494300009PubMedID: 19539751Scopus ID: 2-s2.0-68549128495OAI: oai:DiVA.org:hh-48851DiVA, id: diva2:1719017
Note
Funding text: This work was supported by grants from the DiMI (LSHB-CT-2005-512146), the Research Council of Norway, the Swedish Research Council, the Swedish Strategic Science foundation, and the Throne Holst Foundation.
2022-12-142022-12-142023-02-15Bibliographically approved